A squishy worm that starts its life as something of a floating head in the Pacific Ocean is changing what scientists know about metamorphosis at the cellular level.Unlike humans, about 80% of animal species undergo metamorphosis, a stepped development from egg to larva to adult, but how it works at a cellular level is not well understood. Some theories and prior research suggested that the original cells in the larva die and are replaced with newly generated adult cells. Other work pointed to cells growing into their same function—for example, larval skin cells would become adult skin cells.
Instead, a Stanford-led study has found strong evidence in an acorn worm called Schizocardium californicum that most larval cells were reprogrammed, with even neurons taking on a new role in the adult organism.
“Reprogramming is a bit of an exotic fruit in developmental biology,” said Christopher Lowe, senior author on the study and biology professor in the Stanford School of Humanities and Sciences. “Generally, we used to think that as cells develop, they become increasingly restricted in their function. But when we start looking at more animals that go through metamorphosis, they may reveal that reprogramming is a much more common feature of development.”
Cellular reprogramming is thought to happen after an injury, or in some species that regenerate organs or whole limbs—but not as a feature of normal development. This study, published in Nature Communications, is the first known research to suggest extensive cellular reprogramming during normal development in an animal with a bilateral body plan, where one side of the body matches the other, as in humans. Previous research has found some of this developmental type of reprogramming in sponges and jellyfish, two organisms that are far from humans on the evolutionary tree. In contrast, these acorn worms are part of the hemichordata phylum, considered an evolutionary link to vertebrate animals, including all mammals.
Following the cells
For this study, the team, led by first author Paul Bump, a former doctoral student in Lowe’s lab at Stanford’s Hopkins Marine Station, conducted genetic analyses on more than 87,000 cells from these acorn worms. The researchers performed single cell RNA sequencing on samples from worms in five developmental stages: early and late larvae, metamorphosis, and early and late juvenile. Using this information, they categorized the cells into 12 classes, such as cartilage, immune, and skin cells.
This analysis found that many larval cells were more similar to each other than they were to the adult cells performing the same function. For example, larval neurons were more like larval gut cells than they were to adult neurons. This was true for more than half of the cells, suggesting that there had been extensive reprogramming. There were some exceptions. For instance, the functions of muscle cells and mesoderm cells, which make up some organs, stayed the same from larval to juvenile stages.
Single-cell sequencing reveals the broad diversity of hemichordate cell types

A UMAP embedding of the cell classes of S. californicum; 55 clusters were identified and 12 cell classes were described. B Selected markers of cell classes of S. californicum, percentage of gene maximum was calculated by taking the mean normalized expression of the gene of interest and dividing by the maximum for any cell class. C–T HCR signal in magenta, nuclei are in gray, scale bars are 100 µm. Each HCR experiment was imaged in triplicate. C foxA HCR expression in early larva. D foxA HCR expression in early juvenile. E fabp6 HCR expression in early larva. F co9a1 HCR expression in late larva. G co9a1 HCR expression in early juvenile. H mox HCR expression in early larva. I mox HCR expression in late larvae. J myl HCR expression during metamorphosis. I myl HCR expression in early juvenile. L cthr expression in early larva. M syt1 HCR expression in early larva. N TH HCR expression in early larva. O TH HCR expression in early juvenile. P pk1l2 HCR expression in early larva. Q cnbd2 HCR expression in early larva. R muc2 HCR expression in early juvenile. S amy1 HCR expression in early larvae. T arsi HCR expression in late larvae. U arsi HCR expression during metamorphosis. V arsi HCR expression in early juvenile.
Bump was also able to place a label, a type of persistent dye, on some larval cells before metamorphosis and follow them through the process to see that they persisted in the adult organism.
“This suggested that cells were not large-scale dying; they were actually being carried over,” Lowe said. “Based on their RNA sequence data, we saw that they had become very different in cell type, which was supportive of the idea that larval cells were being reprogrammed into new fates during metamorphosis, which goes against what most of the field would have predicted.”
An unusual animal for an unusual discovery
Working with the Schizocardium californicum was a challenge. It is not a species used often for research, which meant the scientists had to adapt tools and techniques normally used for other animals.
But the fact that this worm is not usually studied is exactly why it is of interest to the Lowe team. His lab specializes in “non-model” marine organisms as they may reveal more about not just their own development, but also the larger evolutionary history of many animals.
Most model organisms—the types of animals typically used in research, such as mice and zebra fish—are direct developers. They grow directly from an egg or embryo into an adult. These animals are more frequently studied partly because they are closer to humans genetically and partly because direct development is easier to manage in a lab.
Yet the focus on direct development leaves a huge gap in knowledge about the larger animal world, Lowe said, since so many animals are indirect developers that have a larval stage and undergo metamorphosis before growing into an adult.
The Schizocardium californicum worm also has a cousin that is a well-studied direct developer: Saccoglossus kowalevskii, sometimes called the Virginia acorn worm.
There are key differences between the way the two acorn worms develop, which is apparent from observation: When the Virginia acorn worm hatches from an egg, it has the worm-like shape it will have its entire life , while the young larva of the Schizocardium californicum looks nothing like its adult form. This study also suggests that the California worm’s incredible transition is inside and out.
“You can watch this process of metamorphosis and see physically how things radically change, but this morphological transformation is also mirrored by a massive change in cellular components,” Lowe said.
Source – Stanford University
A squishy worm that starts its life as something of a floating head in the Pacific Ocean is changing what scientists know about metamorphosis at the cellular level.Unlike humans, about 80% of animal species undergo metamorphosis, a stepped development from egg to larva to adult, but how it works at a cellular level is not well understood. Some theories and prior research suggested that the original cells in the larva die and are replaced with newly generated adult cells. Other work pointed to cells growing into their same function—for example, larval skin cells would become adult skin cells.
Instead, a Stanford-led study has found strong evidence in an acorn worm called Schizocardium californicum that most larval cells were reprogrammed, with even neurons taking on a new role in the adult organism.
Cellular reprogramming is thought to happen after an injury, or in some species that regenerate organs or whole limbs—but not as a feature of normal development. This study, published in Nature Communications, is the first known research to suggest extensive cellular reprogramming during normal development in an animal with a bilateral body plan, where one side of the body matches the other, as in humans. Previous research has found some of this developmental type of reprogramming in sponges and jellyfish, two organisms that are far from humans on the evolutionary tree. In contrast, these acorn worms are part of the hemichordata phylum, considered an evolutionary link to vertebrate animals, including all mammals.
Following the cells
For this study, the team, led by first author Paul Bump, a former doctoral student in Lowe’s lab at Stanford’s Hopkins Marine Station, conducted genetic analyses on more than 87,000 cells from these acorn worms. The researchers performed single cell RNA sequencing on samples from worms in five developmental stages: early and late larvae, metamorphosis, and early and late juvenile. Using this information, they categorized the cells into 12 classes, such as cartilage, immune, and skin cells.
This analysis found that many larval cells were more similar to each other than they were to the adult cells performing the same function. For example, larval neurons were more like larval gut cells than they were to adult neurons. This was true for more than half of the cells, suggesting that there had been extensive reprogramming. There were some exceptions. For instance, the functions of muscle cells and mesoderm cells, which make up some organs, stayed the same from larval to juvenile stages.
Single-cell sequencing reveals the broad diversity of hemichordate cell types
A UMAP embedding of the cell classes of S. californicum; 55 clusters were identified and 12 cell classes were described. B Selected markers of cell classes of S. californicum, percentage of gene maximum was calculated by taking the mean normalized expression of the gene of interest and dividing by the maximum for any cell class. C–T HCR signal in magenta, nuclei are in gray, scale bars are 100 µm. Each HCR experiment was imaged in triplicate. C foxA HCR expression in early larva. D foxA HCR expression in early juvenile. E fabp6 HCR expression in early larva. F co9a1 HCR expression in late larva. G co9a1 HCR expression in early juvenile. H mox HCR expression in early larva. I mox HCR expression in late larvae. J myl HCR expression during metamorphosis. I myl HCR expression in early juvenile. L cthr expression in early larva. M syt1 HCR expression in early larva. N TH HCR expression in early larva. O TH HCR expression in early juvenile. P pk1l2 HCR expression in early larva. Q cnbd2 HCR expression in early larva. R muc2 HCR expression in early juvenile. S amy1 HCR expression in early larvae. T arsi HCR expression in late larvae. U arsi HCR expression during metamorphosis. V arsi HCR expression in early juvenile.
Bump was also able to place a label, a type of persistent dye, on some larval cells before metamorphosis and follow them through the process to see that they persisted in the adult organism.
An unusual animal for an unusual discovery
Working with the Schizocardium californicum was a challenge. It is not a species used often for research, which meant the scientists had to adapt tools and techniques normally used for other animals.
But the fact that this worm is not usually studied is exactly why it is of interest to the Lowe team. His lab specializes in “non-model” marine organisms as they may reveal more about not just their own development, but also the larger evolutionary history of many animals.
Most model organisms—the types of animals typically used in research, such as mice and zebra fish—are direct developers. They grow directly from an egg or embryo into an adult. These animals are more frequently studied partly because they are closer to humans genetically and partly because direct development is easier to manage in a lab.
Yet the focus on direct development leaves a huge gap in knowledge about the larger animal world, Lowe said, since so many animals are indirect developers that have a larval stage and undergo metamorphosis before growing into an adult.
The Schizocardium californicum worm also has a cousin that is a well-studied direct developer: Saccoglossus kowalevskii, sometimes called the Virginia acorn worm.
There are key differences between the way the two acorn worms develop, which is apparent from observation: When the Virginia acorn worm hatches from an egg, it has the worm-like shape it will have its entire life , while the young larva of the Schizocardium californicum looks nothing like its adult form. This study also suggests that the California worm’s incredible transition is inside and out.
Source – Stanford University
Bump P, Brewster C, Formery L, Lubeck L, Campbell C, Morri M, Sit R, Rokhsar DS, Benham-Pyle B, Sánchez Alvarado A, Lowe CJ. (2026) Distinct cell states define larval and adult body plans in a hemichordate. Nature Communications 17: 9358. [article]
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A squishy worm that starts its life as something of a floating head in the Pacific Ocean is changing what scientists know about metamorphosis at the cellular level.Unlike humans, about 80% of animal species undergo metamorphosis, a stepped development from egg to larva to adult, but how it works at a cellular level is not well understood. Some theories and prior research suggested that the original cells in the larva die and are replaced with newly generated adult cells. Other work pointed to cells growing into their same function—for example, larval skin cells would become adult skin cells.
Instead, a Stanford-led study has found strong evidence in an acorn worm called Schizocardium californicum that most larval cells were reprogrammed, with even neurons taking on a new role in the adult organism.
Cellular reprogramming is thought to happen after an injury, or in some species that regenerate organs or whole limbs—but not as a feature of normal development. This study, published in Nature Communications, is the first known research to suggest extensive cellular reprogramming during normal development in an animal with a bilateral body plan, where one side of the body matches the other, as in humans. Previous research has found some of this developmental type of reprogramming in sponges and jellyfish, two organisms that are far from humans on the evolutionary tree. In contrast, these acorn worms are part of the hemichordata phylum, considered an evolutionary link to vertebrate animals, including all mammals.
Following the cells
For this study, the team, led by first author Paul Bump, a former doctoral student in Lowe’s lab at Stanford’s Hopkins Marine Station, conducted genetic analyses on more than 87,000 cells from these acorn worms. The researchers performed single cell RNA sequencing on samples from worms in five developmental stages: early and late larvae, metamorphosis, and early and late juvenile. Using this information, they categorized the cells into 12 classes, such as cartilage, immune, and skin cells.
This analysis found that many larval cells were more similar to each other than they were to the adult cells performing the same function. For example, larval neurons were more like larval gut cells than they were to adult neurons. This was true for more than half of the cells, suggesting that there had been extensive reprogramming. There were some exceptions. For instance, the functions of muscle cells and mesoderm cells, which make up some organs, stayed the same from larval to juvenile stages.
Single-cell sequencing reveals the broad diversity of hemichordate cell types
A UMAP embedding of the cell classes of S. californicum; 55 clusters were identified and 12 cell classes were described. B Selected markers of cell classes of S. californicum, percentage of gene maximum was calculated by taking the mean normalized expression of the gene of interest and dividing by the maximum for any cell class. C–T HCR signal in magenta, nuclei are in gray, scale bars are 100 µm. Each HCR experiment was imaged in triplicate. C foxA HCR expression in early larva. D foxA HCR expression in early juvenile. E fabp6 HCR expression in early larva. F co9a1 HCR expression in late larva. G co9a1 HCR expression in early juvenile. H mox HCR expression in early larva. I mox HCR expression in late larvae. J myl HCR expression during metamorphosis. I myl HCR expression in early juvenile. L cthr expression in early larva. M syt1 HCR expression in early larva. N TH HCR expression in early larva. O TH HCR expression in early juvenile. P pk1l2 HCR expression in early larva. Q cnbd2 HCR expression in early larva. R muc2 HCR expression in early juvenile. S amy1 HCR expression in early larvae. T arsi HCR expression in late larvae. U arsi HCR expression during metamorphosis. V arsi HCR expression in early juvenile.
Bump was also able to place a label, a type of persistent dye, on some larval cells before metamorphosis and follow them through the process to see that they persisted in the adult organism.
An unusual animal for an unusual discovery
Working with the Schizocardium californicum was a challenge. It is not a species used often for research, which meant the scientists had to adapt tools and techniques normally used for other animals.
But the fact that this worm is not usually studied is exactly why it is of interest to the Lowe team. His lab specializes in “non-model” marine organisms as they may reveal more about not just their own development, but also the larger evolutionary history of many animals.
Most model organisms—the types of animals typically used in research, such as mice and zebra fish—are direct developers. They grow directly from an egg or embryo into an adult. These animals are more frequently studied partly because they are closer to humans genetically and partly because direct development is easier to manage in a lab.
Yet the focus on direct development leaves a huge gap in knowledge about the larger animal world, Lowe said, since so many animals are indirect developers that have a larval stage and undergo metamorphosis before growing into an adult.
The Schizocardium californicum worm also has a cousin that is a well-studied direct developer: Saccoglossus kowalevskii, sometimes called the Virginia acorn worm.
There are key differences between the way the two acorn worms develop, which is apparent from observation: When the Virginia acorn worm hatches from an egg, it has the worm-like shape it will have its entire life , while the young larva of the Schizocardium californicum looks nothing like its adult form. This study also suggests that the California worm’s incredible transition is inside and out.
Source – Stanford University
Bump P, Brewster C, Formery L, Lubeck L, Campbell C, Morri M, Sit R, Rokhsar DS, Benham-Pyle B, Sánchez Alvarado A, Lowe CJ. (2026) Distinct cell states define larval and adult body plans in a hemichordate. Nature Communications 17: 9358. [article]
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Scientists identify the neuroblastoma cells that signal poor outcomes
Novel biosensor uses DNA ‘barcodes’ to uncover disease signals in cells
CellART extracts single-cell information from high-resolution spatial transcriptomics
Cell2space restores spatial context to single-cell RNA sequencing data
Urine test may improve bladder cancer diagnosis and guide treatment decisions
DeCoRE – a computational method to resolve RNA structural heterogeneity from RNA structure probing data by direct RNA sequencing
Tracing 700 million years of cell evolution
How should biological replicates be handled in long-read RNA sequencing?
RNA-Seq reveals a new way the developing heart controls its growth
The Human RNome Project Consortium seeks to publish first-ever complete sequence of the body’s RNA
scFlowReport brings multiple single-cell RNA sequencing analyses into one workflow
Long-read RNA sequencing reveals how neurons choose alternative RNA endings
DeOPUS improves cell-type estimates from bulk RNA sequencing
ResolVI improves accuracy in spatial transcriptomics analysis
RNA sequencing reveals transcriptional allele differences in prostate cancer stem cells
Unmasking “zombie cells” in aging tissue with an AI-powered barcode
RNA variant imaging for cancer diagnosis
Autism-risk mutations reveal two opposing patterns of brain gene activity
A real-data approach to evaluating RNA transcript analysis methods
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